epi-Inositol

Modify Date: 2024-01-02 05:03:38

epi-Inositol Structure
epi-Inositol structure
Common Name epi-Inositol
CAS Number 488-58-4 Molecular Weight 180.156
Density 2.0±0.1 g/cm3 Boiling Point 291.3±40.0 °C at 760 mmHg
Molecular Formula C6H12O6 Melting Point 304°C(dec.)(lit.)
MSDS Chinese USA Flash Point 143.4±21.9 °C

 Use of epi-Inositol


epi-Inositol is an endogenous metabolite present in Cerebrospinal_Fluid that can be used for the research of Ethanol Consumption[1][2].

 Names

Name epi-Inositol
Synonym More Synonyms

 epi-Inositol Biological Activity

Description epi-Inositol is an endogenous metabolite present in Cerebrospinal_Fluid that can be used for the research of Ethanol Consumption[1][2].
Related Catalog
In Vitro Endogenous metabolites is defined as those that are annotated by Kyoto Encyclopedia of Genes and Genomes as substrates or products of the ~1900 metabolic enzymes encoded in our genome. It is clear in the body of literature that there are documented toxic properties for many of these metabolites[1].
References

[1]. Lee N, et al. Endogenous toxic metabolites and implications in cancer therapy. Oncogene. 2020 Aug;39(35):5709-5720.  

[2]. Viola A, et al. High cerebral scyllo-inositol: a new marker of brain metabolism disturbances induced by chronic alcoholism. MAGMA. 2004 Sep;17(1):47-61.  

 Chemical & Physical Properties

Density 2.0±0.1 g/cm3
Boiling Point 291.3±40.0 °C at 760 mmHg
Melting Point 304°C(dec.)(lit.)
Molecular Formula C6H12O6
Molecular Weight 180.156
Flash Point 143.4±21.9 °C
Exact Mass 180.063385
PSA 121.38000
LogP -2.11
Vapour Pressure 0.0±1.4 mmHg at 25°C
Index of Refraction 1.784
Storage condition 2-8°C

 Safety Information

RIDADR NONH for all modes of transport
HS Code 2906199090

 Synthetic Route

 Customs

HS Code 2906199090
Summary 2906199090. cyclanic, cyclenic or cyclotherpenic alcohols. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

 Articles8

More Articles
Synthesis of allo- and epi-inositol via the NHC-catalyzed carbocyclization of carbohydrate-derived dialdehydes.

J. Org. Chem. 79(11) , 5088-96, (2014)

A synthesis of carbocyclic sugars from carbohydrate-derived dialdehydes using organocatalysis has been developed. Sorbitol, mannitol, and galactitol were converted via 1,6-tritylation, perbenzylation ...

Synthesis of phosphatidylinositols having various inositol stereoisomers by engineered phospholipase D.

J. Biosci. Bioeng. 109(4) , 337-40, (2010)

Phospholipase D-mediated synthesis of phosphatidylinositols having various inositol stereoisomers was studied. Seven inositol stereoisomers were tested, all of which were found to be substrates of the...

Cyclohexanehexol inhibitors of Abeta aggregation prevent and reverse Alzheimer phenotype in a mouse model.

Nat. Med. 12(7) , 801-8, (2006)

When given orally to a transgenic mouse model of Alzheimer disease, cyclohexanehexol stereoisomers inhibit aggregation of amyloid beta peptide (Abeta) into high-molecular-weight oligomers in the brain...

 Synonyms

1,2,3,4,5,6-Cyclohexanehexol, (1α,2α,3α,4α,5α,6β)-
(1R,2R,3r,4S,5S,6s)-1,2,3,4,5,6-Cyclohexanehexol
(1R,2R,3r,4S,5S,6s)-Cyclohexane-1,2,3,4,5,6-hexol
epi-Inositol
1,2,3,4,5/6-Inositol